Facsprep Robotic Sample Preparation System

FDA 510(k) K904795 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK904795

Submission

Device name
Facsprep Robotic Sample Preparation System
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
October 19, 1990
Decision date
December 31, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKH – Apparatus, Automated Blood Cell Diluting
Device class
Class I (low risk)
Regulation
21 CFR 864.5240
Specialty
Hematology

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K022512Cellprep Sample Preparation System, Model 9518GKH · Traditional Immunicon Corp.09/30/2002SE
K021150Coulter CellprepGKH · Traditional Beckman Coulter, Inc.06/11/2002SE
K935953Coulter Multi Q PrepGKH · Traditional Coulter Corp.03/11/1994SE
K923530Coulter Multi-Q-PrepGKH · Traditional Coulter Electronics, Inc.10/14/1992SE
K882767Sysmex DD-100 Whole Blood Dilution SystemGKH · Traditional Toa Medical Electronics USA, Inc.07/18/1988SE
K852373AD150, Automated Hematology DilutorGKH · Traditional Abbott Diagnostics07/05/1985SE
K842747Hycel Dilutor, Various Models/MultiGKH · Traditional R&D Systems, Inc.10/01/1984SE
K842446Dilu-Matic 140GKH · Traditional Abbott Diagnostics09/06/1984SE

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Questions and answers

When was Facsprep Robotic Sample Preparation System cleared by the FDA?

Facsprep Robotic Sample Preparation System (K904795) received a 510(k) decision of Substantially Equivalent on December 31, 1990, 73 days after the submission was received.

What is the product code of K904795?

The FDA product code is GKH – Apparatus, Automated Blood Cell Diluting, a Class I (low risk) device regulated under 21 CFR 864.5240.